"Ruibang Biomedical" Lemp fluorescence analyzer (unsterilized) - Taiwan Registration 52cd3eea9032f0e4ac7c4873ae42e556
Access comprehensive regulatory information for "Ruibang Biomedical" Lemp fluorescence analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 52cd3eea9032f0e4ac7c4873ae42e556 and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RESPONSE BIOMEDICAL CORPORATION, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Fluorescence Instrument for Clinical Use (A.2560)".
A Clinical chemistry and clinical toxicology
A.2560 Fluorometer for clinical use
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Jun 17, 2015
Jun 17, 2025
Sep 30, 2021
Cancellation Information
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